Verified Tech Jobs & Hiring Companies, Updated Every 24 Hours

Job Title Software Technologist I(Python , Linux, AWS) Job Description The Software Development Engineer is responsible for executing comprehensive code reviews to uphold coding standards, pinpoint potential bugs, and advocate for best practices in software development, nurturing a culture of continuous improvement and top-tier code quality. The role assists DevOps in software deployment, ensuring personal performance metrics are achieved, while also defining, monitoring, and meeting broader performance and quality benchmarks. The role identifies and rectifies software defects by analyzing logs, reproducing issues, and implementing effective fixes to bolster software reliability and performance. The role develops and maintains detailed technical documentation, encompassing system architecture diagrams, API specifications, and user guides, to facilitate knowledge sharing and support. The role coaches new joiners and exerts influence within team - local lab/product. Job Responsibilities: • Participates in full software development processes (Python) working with broader autonomy and in pairing mode with other software team members, challenging requirements, design, and quality. • Serves as a recognized technical expert in specific areas within the team, leading the creation of software designs and providing guidance on best practices. • Takes on moderately complex software development tasks, collaborating with senior team members to deliver high-quality software solutions that meet project requirements. • Develops and executes comprehensive test plans, including unit, integration, and system tests, to ensure software reliability, performance, and adherence to specifications. • Conducts thorough code reviews to ensure adherence to coding standards, identify potential bugs, and promote best practices in software development, fostering a culture of continuous improvement and high-quality code. • Supports DevOps in deploying software, setting, monitoring, and ensuring own performance metrics are met, while also defining, monitoring, and meeting broader performance and quality metrics. • Diagnoses and resolves software defects by analyzing logs, reproducing issues, and implementing effective fixes to enhance software reliability and performance. • Creates and maintains comprehensive technical documentation, including system architecture diagrams, API specifications, and user guides to facilitate knowledge sharing and support. • Keeps abreast of emerging technologies, industry trends, and best practices in software development to continuously improve skill sets and apply innovative solutions. • Applies analytical skills to resolve medium complexity requests efficiently, exercising judgment within defined procedures/practices to determine appropriate action. Minimum required Education: Bachelor's Degree in Computer Science, Software Engineering, Information Technology OR Vocational Education in Information Technology or equivalent. Minimum required Experience: Minimum 4 years of experience with engineering Education in areas such as Software Development, (Python) Software Design and Architecture, Testing and Quality Assurance or equivalent. Python, Linux, AWS, Ansible, MongoDB, GitHub Actions, Software Engineering, CICD, git, shell scripts, Powershell scripting, GEn AI Prompting Experience in AWS Environment How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. Indicate if this role is an office/field/onsite role. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. • Learn more about our business . • Discover our rich and exciting history . • Learn more about our purpose . If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here .

Job Title NPSS Quality Assurance Manager Job Description Job Title: NPSS Quality Assurance Manager Lead and execute compliant, risk-based assurance for computerized systems that support medical device quality and business processes. This role combines hands-on Computer System Validation (CSV), quality oversight, stakeholder leadership, and audit readiness across the system lifecycle. Focus CSV / CSA and Quality Assurance Experience 8+ years in regulated environments Work Model Office-based The opportunity As an NPSS QA Manager, you will own and strengthen the validation and assurance framework for non-product software and computerized systems used in a regulated medical device environment. You will partner with process owners, IT, Quality, Regulatory, Cybersecurity, Privacy, suppliers, and project teams to ensure systems are fit for intended use, compliant, inspection-ready, and maintained in a validated state. Your role Provide quality oversight and consultancy across the full computerized system lifecycle, including intended use, classification, validation planning, requirements, risk assessment, supplier assessment, test strategy, traceability, release, change control, periodic review, incident and problem management, and retirement. Develop, implement, and maintain computerized system validation deliverables, procedures, and guidance for CSV and Computer Software Assurance (CSA). Collaborate effectively with project teams and the NPSS team, consistently applying current GxP standards. Apply a risk-based, critical-thinking approach that scales assurance activities to patient safety, product quality, data integrity, regulatory, and business risk. Author, review, and approve validation and assurance deliverables, including validation plans, requirements and specifications, risk assessments, protocols or test evidence, traceability documentation, deviations, reports, and validation summaries. Ensure electronic records, electronic signatures, audit trails, access controls, data migration, interfaces, backup and restore, and data integrity controls are appropriately assessed and verified where applicable. Advise projects using Agile, DevOps, cloud, SaaS, configurable platforms, ERP, QMS, manufacturing, analytics, and other enterprise applications on compliant lifecycle controls and objective evidence. Assess and leverage supplier documentation and automated testing evidence where justified through documented risk and quality decisions. Ensure validated systems remain in a controlled state through change impact assessments, periodic reviews, issue and CAPA management, and lifecycle monitoring. Prepare for and support internal audits, external audits, and regulatory inspections. Present validation strategies and evidence and coordinate clear, timely responses to observations. Lead cross-functional resolution of complex quality and compliance issues, facilitate risk-based decisions, and escalate significant compliance risks when needed. Drive measurable improvements in validation efficiency, right-first-time quality, standardization, automation, and inspection readiness without weakening compliance controls. Coach and mentor validation engineers, validation leads, system owners, testers, and project team members, and develop or deliver role-based training on lifecycle and assurance requirements. You are the right fit if you have Bachelor’s or master’s degree in engineering, computer science, information systems, life sciences, quality, or a related technical field, or equivalent relevant experience. Minimum 8-12 years of relevant experience in computerized systems, software quality, validation, quality assurance, or quality systems within medical devices, pharmaceutical, biotechnology, diagnostics, or another highly regulated life sciences industry. Demonstrable hands-on experience planning, authoring, executing, reviewing, and approving CSV or CSA deliverables for complex computerized systems. Strong working knowledge of risk-based validation, data integrity, electronic records and signatures, configuration and change control, supplier assurance, and maintaining systems in a validated state. Experience supporting audits or inspections and explaining and defending validation strategies, risk decisions, and objective evidence to auditors or regulators. Ability to translate regulatory and quality requirements into practical controls for business, IT, and project teams. Excellent technical writing, facilitation, stakeholder management, and verbal communication skills in English. Ability to influence without direct authority, manage competing priorities, and make well-reasoned quality decisions in a matrix organization. Regulatory and industry knowledge Candidates should bring practical knowledge of several of the following, with depth appropriate to the systems and markets supported: FDA Quality System Regulation / Quality Management System Regulation, including controls applicable to production and quality system software; 21 CFR Part 11 and EU GMP Annex 11 principles for electronic records, electronic signatures, and computerized systems, where applicable; ISO 13485 quality management system requirements and data integrity expectations; FDA Computer Software Assurance guidance and risk-based assurance concepts; ISPE GAMP 5 (A Risk-Based Approach to Compliant GxP Computerized Systems) principles and recognized good practices for computerized system lifecycle management; Agile and DevOps delivery models, cloud and SaaS platforms, automated testing, and supplier-managed services. Preferred qualifications Hands-on experience validating enterprise platforms such as ERP, eQMS, PLM, MES, LIMS, CRM, data and analytics platforms, or regulated workflow applications. Experience working with validation workstreams, governance forums, remediation programs, or global process improvement initiatives. Professional certification or formal training in quality, auditing, software quality, validation, risk management, or project management. Experience with requirements, test management, electronic validation lifecycle management, or automated testing tools. What success looks like Validation strategies and deliverables are proportionate to risk, complete, traceable, and accepted right first time. Projects receive early, practical quality guidance and avoid late compliance rework. Systems remain inspection-ready and in a validated state throughout their operational life. Audit and inspection questions are answered clearly with readily available, defensible evidence. Project teams adopt consistent, efficient assurance practices and demonstrate increased capability. How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. • Learn more about our business . • Discover our rich and exciting history . • Learn more about our purpose . If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here .

Job Title NPSS Quality Assurance Manager Job Description Job Title: NPSS Quality Assurance Manager Lead and execute compliant, risk-based assurance for computerized systems that support medical device quality and business processes. This role combines hands-on Computer System Validation (CSV), quality oversight, stakeholder leadership, and audit readiness across the system lifecycle. Focus CSV / CSA and Quality Assurance Experience 8+ years in regulated environments Work Model Office-based The opportunity As an NPSS QA Manager, you will own and strengthen the validation and assurance framework for non-product software and computerized systems used in a regulated medical device environment. You will partner with process owners, IT, Quality, Regulatory, Cybersecurity, Privacy, suppliers, and project teams to ensure systems are fit for intended use, compliant, inspection-ready, and maintained in a validated state. Your role Provide quality oversight and consultancy across the full computerized system lifecycle, including intended use, classification, validation planning, requirements, risk assessment, supplier assessment, test strategy, traceability, release, change control, periodic review, incident and problem management, and retirement. Develop, implement, and maintain computerized system validation deliverables, procedures, and guidance for CSV and Computer Software Assurance (CSA). Collaborate effectively with project teams and the NPSS team, consistently applying current GxP standards. Apply a risk-based, critical-thinking approach that scales assurance activities to patient safety, product quality, data integrity, regulatory, and business risk. Author, review, and approve validation and assurance deliverables, including validation plans, requirements and specifications, risk assessments, protocols or test evidence, traceability documentation, deviations, reports, and validation summaries. Ensure electronic records, electronic signatures, audit trails, access controls, data migration, interfaces, backup and restore, and data integrity controls are appropriately assessed and verified where applicable. Advise projects using Agile, DevOps, cloud, SaaS, configurable platforms, ERP, QMS, manufacturing, analytics, and other enterprise applications on compliant lifecycle controls and objective evidence. Assess and leverage supplier documentation and automated testing evidence where justified through documented risk and quality decisions. Ensure validated systems remain in a controlled state through change impact assessments, periodic reviews, issue and CAPA management, and lifecycle monitoring. Prepare for and support internal audits, external audits, and regulatory inspections. Present validation strategies and evidence and coordinate clear, timely responses to observations. Lead cross-functional resolution of complex quality and compliance issues, facilitate risk-based decisions, and escalate significant compliance risks when needed. Drive measurable improvements in validation efficiency, right-first-time quality, standardization, automation, and inspection readiness without weakening compliance controls. Coach and mentor validation engineers, validation leads, system owners, testers, and project team members, and develop or deliver role-based training on lifecycle and assurance requirements. You are the right fit if you have Bachelor’s or master’s degree in engineering, computer science, information systems, life sciences, quality, or a related technical field, or equivalent relevant experience. Minimum 8-12 years of relevant experience in computerized systems, software quality, validation, quality assurance, or quality systems within medical devices, pharmaceutical, biotechnology, diagnostics, or another highly regulated life sciences industry. Demonstrable hands-on experience planning, authoring, executing, reviewing, and approving CSV or CSA deliverables for complex computerized systems. Strong working knowledge of risk-based validation, data integrity, electronic records and signatures, configuration and change control, supplier assurance, and maintaining systems in a validated state. Experience supporting audits or inspections and explaining and defending validation strategies, risk decisions, and objective evidence to auditors or regulators. Ability to translate regulatory and quality requirements into practical controls for business, IT, and project teams. Excellent technical writing, facilitation, stakeholder management, and verbal communication skills in English. Ability to influence without direct authority, manage competing priorities, and make well-reasoned quality decisions in a matrix organization. Regulatory and industry knowledge Candidates should bring practical knowledge of several of the following, with depth appropriate to the systems and markets supported: FDA Quality System Regulation / Quality Management System Regulation, including controls applicable to production and quality system software; 21 CFR Part 11 and EU GMP Annex 11 principles for electronic records, electronic signatures, and computerized systems, where applicable; ISO 13485 quality management system requirements and data integrity expectations; FDA Computer Software Assurance guidance and risk-based assurance concepts; ISPE GAMP 5 (A Risk-Based Approach to Compliant GxP Computerized Systems) principles and recognized good practices for computerized system lifecycle management; Agile and DevOps delivery models, cloud and SaaS platforms, automated testing, and supplier-managed services. Preferred qualifications Hands-on experience validating enterprise platforms such as ERP, eQMS, PLM, MES, LIMS, CRM, data and analytics platforms, or regulated workflow applications. Experience working with validation workstreams, governance forums, remediation programs, or global process improvement initiatives. Professional certification or formal training in quality, auditing, software quality, validation, risk management, or project management. Experience with requirements, test management, electronic validation lifecycle management, or automated testing tools. What success looks like Validation strategies and deliverables are proportionate to risk, complete, traceable, and accepted right first time. Projects receive early, practical quality guidance and avoid late compliance rework. Systems remain inspection-ready and in a validated state throughout their operational life. Audit and inspection questions are answered clearly with readily available, defensible evidence. Project teams adopt consistent, efficient assurance practices and demonstrate increased capability. How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. • Learn more about our business . • Discover our rich and exciting history . • Learn more about our purpose . If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here .

Job Title Software Technologist I - C# .NET Full Stack Job Description Philips is a global leader in health technology, dedicated to improving lives through meaningful innovation. This role sits within Hospital Patient Monitoring (HPM) , which provides advanced monitoring solutions for acute care settings. From bedside and transport monitors to centralized systems, HPM helps clinicians identify at-risk patients and intervene quickly. The position is based in Bangalore, a key hub supporting innovation and collaboration across Philips. Your role: Participate in the full software development lifecycle, from requirements analysis to deployment Design and develop scalable, secure, and maintainable applications using C# and .NET technologies Implement front-end components and integrate them with backend services Develop and execute unit, integration, and system tests to ensure quality and reliability Conduct code reviews to maintain coding standards and best practices Collaborate with DevOps teams for deployment and monitoring Diagnose and resolve software defects, ensuring optimal performance Create and maintain technical documentation (architecture diagrams, API specs, user guides) Stay updated on emerging technologies and apply innovative solutions Mentor junior developers and contribute to a culture of continuous improvement. You're the right fit if: Experience: Bachelor's Degree i n Computer Science, Software Engineering, Information Technology 5–8 years as a Full Stack Developer with strong C# expertise Core Skills: Proficient in C# language fundamentals and OOP concepts (classes, interfaces, inheritance, LINQ, async/await, exception handling) Hands-on experience with ASP.NET Core for backend development Strong understanding of RESTful API design and implementation Front-end proficiency in HTML, CSS, JavaScript, and frameworks like Angular, React, or Node.js Familiarity with UI/UX principles and responsive design Database & Integration: Experience with MS SQL Server or PostgreSQL Knowledge of Entity Framework, database migrations, and query optimization. Awareness of SMTP, SNMP, and observability frameworks (good to have) Cloud & DevOps: Experience with AWS or Azure Familiarity with CI/CD pipelines and tools (e.g., GitHub Actions) Skilled in Docker and containerized deployments Understanding of microservices architecture and Kubernetes (preferred) Additional: Comfortable working in Agile/Scrum environments Strong debugging and troubleshooting skills Excellent communication and collaboration abilities How we work together We believe that we are better together than apart. This is an office-based role, which means working in person at least 3 days per week. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. • Learn more about our business . • Discover our rich and exciting history . • Learn more about our purpose . If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here . #LI-PH1 #LI-OFFICE #ConnectedCare